Cytological Diagnosis of Giant Cell Lesions in Infants-A Red Herring

D. Nath
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Abstract

Introduction: Head and neck swellings and nodules are commonly seen in the pediatric population with most of the lesions falling in the benign neoplasm category. Auricular tumors are relatively rare with most common swellings being infective or congenital. Giant cell mesenchymal tumors are an entire spectrum of tumors and they are rarely been reported on the pinna. Pilomatricoma is an unusual, relatively rare, slowly growing benign tumor of the skin appendages. The histomorphological features of pilomatricoma are characteristic, but the cytological diagnosis remains problematic because of mimickers with other small round blue cell tumors. Here we present a case of pilomatricoma which presented with diagnostic pitfall in cytological diagnosis Case: A two-and-a-half-month-old female child presented with a slowly growing fleshy pinkish whitish firm swelling at the medial aspect of the right pinna for last 1 month. The swelling was painless and was not associated with other symptoms like fever, discharge from the lesion or external ear, any hearing loss or ulceration and destruction of the surrounding area. FNAC was done and scant blood mixed material aspirated. Smears showed presence of few clusters of mononuclear round blue cells with few spindled cells with fair number of giant cells admixed with very scant amorphous pink material on a hemorrhagic background. A diagnosis of giant cell mesenchymal lesion was made, and histopathology was advised. Histopathological examination revealed presence of giant cells against intradermal keratin admixed with ghost cells and basaloid to mononuclear intermediate cells. A diagnosis of pilomatricoma was made. Conclusion: The case highlights how giant cells on cytology may masquerade as giant cell mesenchymal lesion in a classic case of pilomatricoma from an uncommon location like pinna in a pediatric patient and may act as a diagnostic pitfall for the cytologist.
婴儿巨细胞病变的细胞学诊断——转移话题
头颈部肿胀和结节常见于儿科人群,大多数病变属于良性肿瘤类别。耳廓肿瘤是相对罕见的,大多数常见的肿胀是感染性或先天性的。巨细胞间充质瘤是一种全谱的肿瘤,在耳廓上很少有报道。毛瘤是一种不寻常的、相对罕见的、生长缓慢的皮肤附属物良性肿瘤。毛瘤的组织形态学特征是特征性的,但细胞学诊断仍有问题,因为它与其他小的圆形蓝色细胞肿瘤相似。我们在此报告一例在细胞学诊断中出现诊断缺陷的头毛瘤病例:一个两个半月大的女婴,在右耳廓内侧缓慢生长的肉质粉白色硬肿,持续1个月。肿胀是无痛的,没有其他症状,如发烧,从病变或外耳分泌物,任何听力丧失或溃疡和周围区域的破坏。行FNAC,抽吸少量混合血。涂片示出血性背景上有少量单核圆形蓝色细胞团,有少量纺锤形细胞和相当数量的巨细胞,并伴有少量无定形粉红色物质。诊断为巨细胞间质病变,建议行组织病理学检查。组织病理学检查显示有对抗皮内角蛋白的巨细胞、鬼影细胞和基底样细胞混合到单核中间细胞。诊断为毛瘤。结论:该病例强调了在一个罕见部位(如儿童患者的耳廓)的典型病例中,细胞学上的巨细胞可能伪装成巨细胞间充质病变,并可能成为细胞学家的诊断陷阱。
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